Description Usage Arguments Examples
produce a filtered RNA-haplotype table as GRanges, limiting to SNP-sets of specific cardinality and (optionally) providing a set of gene ranges 'nearest' to the initial SNP
1 2 3 | filter_haptab(haptab = BiocRnaHap::NA06986_rnahaps,
genegr = ensembldb::genes(EnsDb.Hsapiens.v75::EnsDb.Hsapiens.v75),
varnum_to_use = 2:6, useNearestRubric = FALSE)
|
haptab |
data.frame corresponding to phaser haplotypes.txt table |
genegr |
a GRanges with gene ranges |
varnum_to_use |
the values of the 'variants' field for which records are retained |
useNearestRubric |
logical(1) defaults to FALSE |
1 |
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